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The study was performed on several samples from different parts of the sculpture by means of optical microscopy under visible illumination, Scanning Electron Microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (SEM-EDX) and Gas chromatography mass spectrometry (GC-MS).
Wounding was performed with a pulsed UV laser (355 nm) using a UGA-40 spot illumination scanning system (Rapp OptoElectronic, Germany) fitted to the line-scanning confocal microscope.
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Open image in new window Fig. 5 I V curves for PEC water oxidation of the BiVO4 films measured in 0.1 M KH2PO4 electrolyte under AM1.5G illumination Open image in new window Fig. 6 I V curves of BiVO4 electrodes measured in a 0.1 M phosphate buffer (pH 7) containing 0.1 M Na2SO3 as hole scavenger under AM1.5G, 100 mW cm−2 illumination (scan rate, 50 mV s−1).
Through flat Gauss illumination in scanning direction, pulse quantization effect could be reduced effectively.
AO flood illumination and scanning laser ophthalmoscopy (SLO) have been used to study many properties of the cones, such as: arrangement and packing in normal and defective retinas; changes in reflectance over time; and sampling of the ocular image.
Scanning illumination systems provide for a powerful and flexible means of controlling illumination coherence properties.
The device produces flat Gauss illumination directly at the scanning slit.
By scanning the illumination line across the sample, a 3D OCT image could be collected.
Scanning the illumination point across the tissue in one direction generates a 2D cross-sectional image of the sample (B-scan).
In X-ray ptychography, coherent diffraction patterns are generated by using a spatially confined illumination, which is scanned across the sample such that there is sufficient overlap of adjacent spots illumination footprint.
With scanned illumination, therefore, the rate-limiting step is the shot noise or the photodamage, not the resolution of the data acquisition system.
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